USDA’s Proposed Bioengineered Food Disclosure Rule – A Webinar

Understand the Key Requirements of USDA’s Proposed Bioengineered Food Disclosure Rule

Event Information
Product Format
Prerecorded Event
Presenter(s)
Conference Date
Thu, Jul 12, 2018
Length
60 minutes
Product Description

Get up to Speed with USDA’s Proposed Bioengineered Food Disclosure Rule


The United States Department of Agriculture (USDA) recently proposed a Bioengineered Food Disclosure rule, which provides food companies with guidance on ways to label products made with genetically modified ingredients and identifies which products are covered. This important USDA proposal implements the National Bioengineered Food Disclosure Law of 2016 – and will impact most food companies and their products. Do you understand the key requirements of the proposed rule – and how it will impact you?

Join this session with regulatory consultant, Norma Skolnik, who will help you understand the key requirements of the National Bioengineered Food Disclosure Proposed Rule – such as the ingredients subject to disclosure, the acceptable labeling methods, GMO labeling symbols, thresholds and exemptions, timelines and more.

Skolnik will provide citations to all relevant USDA and FDA laws and regulations, as well as relevant website references and comment submission information, and the know-how tips on how to implement this important new proposed regulation.

Session Highlights

Through this information-packed session, you will learn about:

  • Ingredients subject to disclosure
  • Acceptable labeling methods of disclosure and symbols
  • GMO disclosure symbols that may be used
  • Thresholds of bioengineered foods and exemptions
  • Timelines for implementation of the proposed rule

Who Should Attend

  • Regulatory affairs managers and regulatory associates in the food industry
  • Food marketing managers
  • Food company product managers
  • Anyone involved in food labeling

Ask a question at the Q&A session following the live event and get advice unique to your situation, directly from our expert speaker.

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1-866-458-2965

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1-919-287-2643

About Our Speaker

Norma Skolnik - FDA Regulations Expert

Norma Skolnik has over 35 years of regulatory experience working with the pharmaceutical and dietary supplement industries. She served as Director of Regulatory Affairs for the Americas for Cadbury Adams. Prior to that, she was Director of Regulatory Affairs for the Adams Division of Pfizer and Associate Director of Regulatory Affairs for the Warner-Lambert company. She also served as Director of Regulatory Affairs for Lederle Consumer Healthcare and...   More Info
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